JPH0848963A - シリコーン系感圧接着剤組成物 - Google Patents

シリコーン系感圧接着剤組成物

Info

Publication number: JPH0848963A
Authority: JP; Japan
Prior art keywords: group; resin; sio; mixture; weight
Prior art date: 1994-06-20
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP7153347A

Other languages

English (en)

Japanese (ja)

Inventor

Michael R Strong

レイモンドストロングマイケル

Martin Eric Cifuentes

エリックシフェンテスマーティン

Bernard Vanwert

バンワートバーナード

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Dow Silicones Corp

Original Assignee

Dow Corning Corp

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1994-06-20

Filing date

1995-06-20

Publication date

1996-02-20

1995-06-20 Application filed by Dow Corning Corp filed Critical Dow Corning Corp

1996-02-20 Publication of JPH0848963A publication Critical patent/JPH0848963A/ja

Status Pending legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 105
239000013464 silicone adhesive Substances 0.000 title 1
229920005989 resin Polymers 0.000 claims abstract description 65
239000011347 resin Substances 0.000 claims abstract description 65
-1 siloxane unit Chemical group 0.000 claims abstract description 41
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 26
229910000077 silane Inorganic materials 0.000 claims abstract description 26
229920005645 diorganopolysiloxane polymer Polymers 0.000 claims abstract description 22
150000002430 hydrocarbons Chemical class 0.000 claims abstract description 17
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 16
229920001296 polysiloxane Polymers 0.000 claims abstract description 15
239000007787 solid Substances 0.000 claims abstract description 10
229930195733 hydrocarbon Natural products 0.000 claims abstract description 8
239000004820 Pressure-sensitive adhesive Substances 0.000 claims abstract description 7
239000004215 Carbon black (E152) Substances 0.000 claims abstract description 5
239000007795 chemical reaction product Substances 0.000 claims abstract description 5
239000007788 liquid Substances 0.000 claims abstract description 5
239000000178 monomer Substances 0.000 claims abstract description 4
239000003054 catalyst Substances 0.000 claims description 26
125000004432 carbon atom Chemical group C* 0.000 claims description 16
125000003545 alkoxy group Chemical group 0.000 claims description 13
XYJRNCYWTVGEEG-UHFFFAOYSA-N trimethoxy(2-methylpropyl)silane Chemical compound CO[Si](OC)(OC)CC(C)C XYJRNCYWTVGEEG-UHFFFAOYSA-N 0.000 claims description 11
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical group CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 8
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 7
239000000945 filler Substances 0.000 claims description 7
229910004283 SiO 4 Inorganic materials 0.000 claims description 6
125000002344 aminooxy group Chemical group [H]N([H])O[*] 0.000 claims description 4
BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 claims description 4
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
125000005647 linker group Chemical group 0.000 claims description 3
PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 claims description 3
OHLUUHNLEMFGTQ-AZXPZELESA-N n-methylacetamide Chemical group C[15NH]C(C)=O OHLUUHNLEMFGTQ-AZXPZELESA-N 0.000 claims description 3
229920000642 polymer Polymers 0.000 claims description 3
ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 claims description 3
XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 claims description 2
BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 2
SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 claims description 2
LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 claims description 2
CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 claims description 2
HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 claims description 2
125000001183 hydrocarbyl group Chemical group 0.000 claims 4
WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 claims 1
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 1
239000000853 adhesive Substances 0.000 abstract description 23
230000001070 adhesive effect Effects 0.000 abstract description 23
229910020388 SiO1/2 Inorganic materials 0.000 abstract description 3
229910020485 SiO4/2 Inorganic materials 0.000 abstract 2
239000012530 fluid Substances 0.000 description 28
239000000463 material Substances 0.000 description 18
239000004033 plastic Substances 0.000 description 15
229920003023 plastic Polymers 0.000 description 15
239000012943 hotmelt Substances 0.000 description 14
229910052751 metal Inorganic materials 0.000 description 14
239000002184 metal Substances 0.000 description 14
239000000047 product Substances 0.000 description 13
239000003039 volatile agent Substances 0.000 description 13
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 12
238000000034 method Methods 0.000 description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 9
UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 8
239000002904 solvent Substances 0.000 description 8
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
238000005481 NMR spectroscopy Methods 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
229910000019 calcium carbonate Inorganic materials 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
125000000524 functional group Chemical group 0.000 description 6
238000010438 heat treatment Methods 0.000 description 6
239000006233 lamp black Substances 0.000 description 6
239000002002 slurry Substances 0.000 description 6
235000021355 Stearic acid Nutrition 0.000 description 5
230000000052 comparative effect Effects 0.000 description 5
239000004205 dimethyl polysiloxane Substances 0.000 description 5
WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 5
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 5
239000008117 stearic acid Substances 0.000 description 5
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical group CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 description 4
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
238000001704 evaporation Methods 0.000 description 4
230000008020 evaporation Effects 0.000 description 4
238000005259 measurement Methods 0.000 description 4
229910052710 silicon Inorganic materials 0.000 description 4
239000008096 xylene Substances 0.000 description 4
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
238000005227 gel permeation chromatography Methods 0.000 description 3
238000002156 mixing Methods 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
150000004756 silanes Chemical class 0.000 description 3
238000012360 testing method Methods 0.000 description 3
KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 2
YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 2
238000002835 absorbance Methods 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
238000009529 body temperature measurement Methods 0.000 description 2
YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 2
ZRHOFLXFAAEXEE-UHFFFAOYSA-J butanoate;titanium(4+) Chemical compound [Ti+4].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O ZRHOFLXFAAEXEE-UHFFFAOYSA-J 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
239000012975 dibutyltin dilaurate Substances 0.000 description 2
239000010408 film Substances 0.000 description 2
FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 2
238000011065 in-situ storage Methods 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000011159 matrix material Substances 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000000126 substance Substances 0.000 description 2
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
OGZPYBBKQGPQNU-DABLZPOSSA-N (e)-n-[bis[[(e)-butan-2-ylideneamino]oxy]-methylsilyl]oxybutan-2-imine Chemical compound CC\C(C)=N\O[Si](C)(O\N=C(/C)CC)O\N=C(/C)CC OGZPYBBKQGPQNU-DABLZPOSSA-N 0.000 description 1
NOGBEXBVDOCGDB-NRFIWDAESA-L (z)-4-ethoxy-4-oxobut-2-en-2-olate;propan-2-olate;titanium(4+) Chemical compound [Ti+4].CC(C)[O-].CC(C)[O-].CCOC(=O)\C=C(\C)[O-].CCOC(=O)\C=C(\C)[O-] NOGBEXBVDOCGDB-NRFIWDAESA-L 0.000 description 1
VTRGCUISDBTZIB-UHFFFAOYSA-N 2-aminooxyacetamide Chemical group NOCC(N)=O VTRGCUISDBTZIB-UHFFFAOYSA-N 0.000 description 1
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 1
KBSDLBVPAHQCRY-UHFFFAOYSA-N 307496-19-1 Chemical group C1CC=CCC1CC[Si](O1)(O2)O[Si](O3)(C4CCCC4)O[Si](O4)(C5CCCC5)O[Si]1(C1CCCC1)O[Si](O1)(C5CCCC5)O[Si]2(C2CCCC2)O[Si]3(C2CCCC2)O[Si]41C1CCCC1 KBSDLBVPAHQCRY-UHFFFAOYSA-N 0.000 description 1
125000006043 5-hexenyl group Chemical group 0.000 description 1
WDJHALXBUFZDSR-UHFFFAOYSA-N Acetoacetic acid Natural products CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
229910052582 BN Inorganic materials 0.000 description 1
229920002799 BoPET Polymers 0.000 description 1
PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
239000005041 Mylar™ Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
229910004298 SiO 2 Inorganic materials 0.000 description 1
229910020175 SiOH Inorganic materials 0.000 description 1
229910002808 Si–O–Si Inorganic materials 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
DCEAIJSAWZPVQY-UHFFFAOYSA-N [SiH4].CO[Si](CCCNCCN)(OC)OC Chemical compound [SiH4].CO[Si](CCCNCCN)(OC)OC DCEAIJSAWZPVQY-UHFFFAOYSA-N 0.000 description 1
DWCBWHINVBESJA-UHFFFAOYSA-N [SiH4].CO[Si](OC)(OC)CCCOCC1CO1 Chemical compound [SiH4].CO[Si](OC)(OC)CCCOCC1CO1 DWCBWHINVBESJA-UHFFFAOYSA-N 0.000 description 1
KXJLGCBCRCSXQF-UHFFFAOYSA-N [diacetyloxy(ethyl)silyl] acetate Chemical compound CC(=O)O[Si](CC)(OC(C)=O)OC(C)=O KXJLGCBCRCSXQF-UHFFFAOYSA-N 0.000 description 1
TVJPBVNWVPUZBM-UHFFFAOYSA-N [diacetyloxy(methyl)silyl] acetate Chemical compound CC(=O)O[Si](C)(OC(C)=O)OC(C)=O TVJPBVNWVPUZBM-UHFFFAOYSA-N 0.000 description 1
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
PXAJQJMDEXJWFB-UHFFFAOYSA-N acetone oxime Chemical compound CC(C)=NO PXAJQJMDEXJWFB-UHFFFAOYSA-N 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
239000002318 adhesion promoter Substances 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
239000010425 asbestos Substances 0.000 description 1
QBLDFAIABQKINO-UHFFFAOYSA-N barium borate Chemical compound [Ba+2].[O-]B=O.[O-]B=O QBLDFAIABQKINO-UHFFFAOYSA-N 0.000 description 1
229910021523 barium zirconate Inorganic materials 0.000 description 1
DQBAOWPVHRWLJC-UHFFFAOYSA-N barium(2+);dioxido(oxo)zirconium Chemical compound [Ba+2].[O-][Zr]([O-])=O DQBAOWPVHRWLJC-UHFFFAOYSA-N 0.000 description 1
239000011324 bead Substances 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
239000002981 blocking agent Substances 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000013522 chelant Substances 0.000 description 1
239000002738 chelating agent Substances 0.000 description 1
229910000423 chromium oxide Inorganic materials 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000013329 compounding Methods 0.000 description 1
239000007799 cork Substances 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
238000004807 desolvation Methods 0.000 description 1
125000005594 diketone group Chemical group 0.000 description 1
FSBVERYRVPGNGG-UHFFFAOYSA-N dimagnesium dioxido-bis[[oxido(oxo)silyl]oxy]silane hydrate Chemical compound O.[Mg+2].[Mg+2].[O-][Si](=O)O[Si]([O-])([O-])O[Si]([O-])=O FSBVERYRVPGNGG-UHFFFAOYSA-N 0.000 description 1
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
238000004821 distillation Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
239000010439 graphite Substances 0.000 description 1
229910002804 graphite Inorganic materials 0.000 description 1
150000008282 halocarbons Chemical group 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
150000004677 hydrates Chemical class 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
FYKBHPZYQWSXTG-UHFFFAOYSA-L iron(2+);octanoate Chemical compound [Fe+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O FYKBHPZYQWSXTG-UHFFFAOYSA-L 0.000 description 1
239000002648 laminated material Substances 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
229910052919 magnesium silicate Inorganic materials 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
ARYZCSRUUPFYMY-UHFFFAOYSA-N methoxysilane Chemical compound CO[SiH3] ARYZCSRUUPFYMY-UHFFFAOYSA-N 0.000 description 1
GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000012768 molten material Substances 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000005375 organosiloxane group Chemical group 0.000 description 1
RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
239000002952 polymeric resin Substances 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920001343 polytetrafluoroethylene Polymers 0.000 description 1
239000004810 polytetrafluoroethylene Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
239000000565 sealant Substances 0.000 description 1
AKLJIUURIIIOLU-UHFFFAOYSA-N silane 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound [SiH4].CO[Si](OC)(OC)CCCOC(=O)C(C)=C AKLJIUURIIIOLU-UHFFFAOYSA-N 0.000 description 1
239000010703 silicon Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229920002050 silicone resin Polymers 0.000 description 1
WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000003860 storage Methods 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Chemical group 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000012209 synthetic fiber Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
238000009864 tensile test Methods 0.000 description 1
239000010409 thin film Substances 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
150000003609 titanium compounds Chemical class 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
238000006227 trimethylsilylation reaction Methods 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
230000003442 weekly effect Effects 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1
239000011787 zinc oxide Substances 0.000 description 1
CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
229910001928 zirconium oxide Inorganic materials 0.000 description 1
GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J183/00—Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Adhesives based on derivatives of such polymers
- C09J183/04—Polysiloxanes
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/28—Non-macromolecular organic substances
- C08L2666/44—Silicon-containing compounds

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Adhesives Or Adhesive Processes (AREA)
Silicon Polymers (AREA)

JP7153347A 1994-06-20 1995-06-20 シリコーン系感圧接着剤組成物 Pending JPH0848963A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US26279294A	1994-06-20	1994-06-20
US262792		1994-06-20

Publications (1)

Publication Number	Publication Date
JPH0848963A true JPH0848963A (ja)	1996-02-20

Family

ID=22999069

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP7153347A Pending JPH0848963A (ja)	1994-06-20	1995-06-20	シリコーン系感圧接着剤組成物

Country Status (5)

Country	Link
US (1)	US5561203A (fr)
EP (1)	EP0688846B1 (fr)
JP (1)	JPH0848963A (fr)
CA (1)	CA2152131A1 (fr)
DE (1)	DE69528613T2 (fr)

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JP2002322363A (ja) *	2001-04-10	2002-11-08	Dow Corning Corp	シリコーン組成物およびそれから製造されるシリコーン接着剤
JP2006503958A (ja) *	2002-10-22	2006-02-02	ダウ・コーニング・コーポレイション	ホットメルト接着剤組成物を製造するための連続プロセス
JP2006316190A (ja) *	2005-05-13	2006-11-24	Shin Etsu Chem Co Ltd	室温硬化性オルガノポリシロキサン組成物
JP2009007553A (ja) *	2007-05-25	2009-01-15	Shin Etsu Chem Co Ltd	室温硬化性オルガノポリシロキサン組成物
JP2009516040A (ja) *	2005-11-15	2009-04-16	テーザ・アクチエンゲゼルシャフト	電子製品を製造する際の接合のための両面接着テープの用途
JP2011525444A (ja) *	2008-06-24	2011-09-22	ダウ・コーニング・コーポレイション	ホットメルト接着剤組成物並びにそれらの製造及び使用のための方法
JP2015021019A (ja) *	2013-07-16	2015-02-02	信越化学工業株式会社	室温硬化性オルガノポリシロキサン組成物の製造方法、前記組成物の硬化物を用いた自動車オイルシール、建築用シーラント、及び電気電子部品
WO2019146523A1 (fr) *	2018-01-24	2019-08-01	ダウ・東レ株式会社	Composition d'agent de revêtement, et procédé de revêtement de structure

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US5837784A (en) *	1996-06-12	1998-11-17	Dow Corning Corporation	Method of making alkoxylated organosilicone resins and the resins produced thereby
GB9724055D0 (en) *	1997-11-15	1998-01-14	Dow Corning Sa	Curable polysiloxane compositions
US6124387A (en) *	1998-12-22	2000-09-26	Adco Products, Inc.	Fast-cure silylated polymer adhesive
WO2001005846A1 (fr) *	1999-07-19	2001-01-25	Loctite Corporation	Compositions de silicone renforcees par de la resine durcissables aux u.v., a l'humidite et a la fois aux u.v. et a l'humidite
US6828355B1 (en)	1999-07-19	2004-12-07	Henkel Corporation	Resin-reinforced UV, moisture and UV/moisture dual curable silicone compositions
WO2002000808A1 (fr) *	2000-06-23	2002-01-03	General Electric Company	Composition silicone adhesive par pression
US7013818B2 (en)	2001-10-18	2006-03-21	Guangdong Esquel Textiles Co. Ltd.	Wrinkle free garment and method of manufacture
US6731051B2 (en) *	2002-04-22	2004-05-04	Osram Sylvania Inc.	Blue incandescent appliance lamp
JP4777591B2 (ja) *	2002-10-25	2011-09-21	信越化学工業株式会社	室温硬化性オルガノポリシロキサン組成物
JP2006291018A (ja) *	2005-04-08	2006-10-26	Shin Etsu Chem Co Ltd	Ｌｅｄ素子封止用硬化性樹脂組成物
CN100487934C (zh) *	2005-04-08	2009-05-13	日亚化学工业株式会社	具有由丝网印刷形成的有机硅树脂层的发光器件
JP4791083B2 (ja) *	2005-05-30	2011-10-12	信越化学工業株式会社	光関連デバイス封止用樹脂組成物およびその硬化物
WO2007011538A2 (fr) *	2005-07-19	2007-01-25	Dow Corning Corporation	Adhesifs par pression et procedes d'elaboration
WO2007084266A2 (fr) *	2006-01-19	2007-07-26	Dow Corning Corporation	Adhésif silicone pour l'adhérence sur des surfaces humides
DE102006011112A1 (de) *	2006-03-08	2007-09-13	Tesa Ag	Selbstklebemasse und ihre Verwendung
CN101657522B (zh) *	2007-04-13	2014-05-07	3M创新有限公司	防静电光学透明的压敏粘合剂
US9228117B2 (en)	2008-01-11	2016-01-05	3M Innovative Properties Company	Stretch releasing optically clear pressure sensitive adhesive
JP5251732B2 (ja) *	2008-06-04	2013-07-31	信越化学工業株式会社	シリコーン粘着剤組成物
DE102008041121A1 (de) *	2008-08-08	2010-02-11	Wacker Chemie Ag	Verfahren zur Herstellung von Formkörpern aus Silikonkautschuk
RU2544702C2 (ru) *	2009-04-24	2015-03-20	Хенкель Корпорейшн	Клеи на основе силикон-акрилового гибридного полимера
JP5784593B2 (ja) *	2009-06-04	2015-09-24	ダウコーニングコーポレーションＤｏｗＣｏｒｎｉｎｇＣｏｒｐｏｒａｔｉｏｎ	建築用膜用途に用いられる吹き付け可能な接着剤組成物
EP2524954A4 (fr) *	2010-01-13	2013-06-12	Dow Corning Toray Co Ltd	Composition adhésive à base de silicone pouvant être recollée, matériau de base en forme de feuille ayant une couche adhésive pouvant être recollée obtenue par durcissement de ladite composition, et utilisation dudit matériau de base comme film protecteur ou feuille de fixation
CN102516924A (zh) *	2011-12-07	2012-06-27	上海应用技术学院	一种导电型的有机硅压敏胶乳液及其制备方法
JP7560442B2 (ja) *	2019-03-29	2024-10-02	ダウ・東レ株式会社	硬化性シリコーン組成物、その硬化物、およびその製造方法

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JPS52119659A (en) *	1976-03-24	1977-10-07	Rhone Poulenc Ind	Storageestable organosilicone compound
JPS61108681A (ja) *	1984-10-29	1986-05-27	ダウ　コーニング　コーポレーシヨン	シリコーン感圧接着剤組成物の製造法
JPH01152180A (ja) *	1987-11-02	1989-06-14	Dow Corning Corp	成形可能な弾性感圧接着剤組成物及びその用途
JPH0481487A (ja) *	1990-07-25	1992-03-16	Shin Etsu Chem Co Ltd	感圧接着剤組成物及びその硬化物
JPH04198269A (ja) *	1990-11-26	1992-07-17	Shin Etsu Chem Co Ltd	室温硬化性オルガノポリシロキサン組成物およびその硬化物
JPH05140458A (ja) *	1991-11-20	1993-06-08	Toray Dow Corning Silicone Co Ltd	湿気硬化型シリコーン粘着剤組成物

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JPH086033B2 (ja) *	1990-07-13	1996-01-24	信越化学工業株式会社	コルク粒バインダー用室温硬化性オルガノポリシロキサン組成物並びにコルク粒硬化物及び成型栓
JPH06329914A (ja) *	1993-05-18	1994-11-29	Toray Dow Corning Silicone Co Ltd	室温硬化性オルガノポリシロキサン組成物およびその製造方法
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US5302671A (en) *	1993-06-11	1994-04-12	Dow Corning Corporation	Moisture-curable compositions containing aminoalkoxy-functional silicone

1995
- 1995-04-13 US US08/479,202 patent/US5561203A/en not_active Expired - Fee Related
- 1995-06-14 EP EP95304112A patent/EP0688846B1/fr not_active Expired - Lifetime
- 1995-06-14 DE DE69528613T patent/DE69528613T2/de not_active Expired - Fee Related
- 1995-06-19 CA CA002152131A patent/CA2152131A1/fr not_active Abandoned
- 1995-06-20 JP JP7153347A patent/JPH0848963A/ja active Pending

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JPS52119659A (en) *	1976-03-24	1977-10-07	Rhone Poulenc Ind	Storageestable organosilicone compound
JPS61108681A (ja) *	1984-10-29	1986-05-27	ダウ　コーニング　コーポレーシヨン	シリコーン感圧接着剤組成物の製造法
JPH01152180A (ja) *	1987-11-02	1989-06-14	Dow Corning Corp	成形可能な弾性感圧接着剤組成物及びその用途
JPH0481487A (ja) *	1990-07-25	1992-03-16	Shin Etsu Chem Co Ltd	感圧接着剤組成物及びその硬化物
JPH04198269A (ja) *	1990-11-26	1992-07-17	Shin Etsu Chem Co Ltd	室温硬化性オルガノポリシロキサン組成物およびその硬化物
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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2002322363A (ja) *	2001-04-10	2002-11-08	Dow Corning Corp	シリコーン組成物およびそれから製造されるシリコーン接着剤
JP2006503958A (ja) *	2002-10-22	2006-02-02	ダウ・コーニング・コーポレイション	ホットメルト接着剤組成物を製造するための連続プロセス
JP2006316190A (ja) *	2005-05-13	2006-11-24	Shin Etsu Chem Co Ltd	室温硬化性オルガノポリシロキサン組成物
JP2009516040A (ja) *	2005-11-15	2009-04-16	テーザ・アクチエンゲゼルシャフト	電子製品を製造する際の接合のための両面接着テープの用途
JP2009007553A (ja) *	2007-05-25	2009-01-15	Shin Etsu Chem Co Ltd	室温硬化性オルガノポリシロキサン組成物
JP2011525444A (ja) *	2008-06-24	2011-09-22	ダウ・コーニング・コーポレイション	ホットメルト接着剤組成物並びにそれらの製造及び使用のための方法
JP2015021019A (ja) *	2013-07-16	2015-02-02	信越化学工業株式会社	室温硬化性オルガノポリシロキサン組成物の製造方法、前記組成物の硬化物を用いた自動車オイルシール、建築用シーラント、及び電気電子部品
WO2019146523A1 (fr) *	2018-01-24	2019-08-01	ダウ・東レ株式会社	Composition d'agent de revêtement, et procédé de revêtement de structure
KR20200110361A (ko) *	2018-01-24	2020-09-23	다우 도레이 캄파니 리미티드	코팅제 조성물 및 구조물의 코팅 방법
JPWO2019146523A1 (ja) *	2018-01-24	2021-01-28	ダウ・東レ株式会社	コーティング剤組成物および構造物のコーティング方法

Also Published As

Publication number	Publication date
DE69528613D1 (de)	2002-11-28
CA2152131A1 (fr)	1995-12-21
EP0688846A2 (fr)	1995-12-27
DE69528613T2 (de)	2003-06-26
EP0688846A3 (fr)	1996-10-30
EP0688846B1 (fr)	2002-10-23
US5561203A (en)	1996-10-01

Legal Events

Date

Code

Title

Description

2004-06-02

A02

Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20040601

Publication	Publication Date	Title
JPH0848963A (ja)	1996-02-20	シリコーン系感圧接着剤組成物
JP3602202B2 (ja)	2004-12-15	水分硬化性のシリコーンホットメルト感圧接着剤組成物
EP0628617B1 (fr)	1998-05-20	Adhésifs thermofusibles, sensibles à la pression et durcissables par l'humidité à base de polysiloxanes
US5302671A (en)	1994-04-12	Moisture-curable compositions containing aminoalkoxy-functional silicone
US4143088A (en)	1979-03-06	Rapidly curable, storage-stable organosilicon compositions
KR910005868B1 (ko)	1991-08-06	폴리아실옥시실란을 함유하고, 금속 수산화물 형태의 촉진제 존재하에 빠르게 탄성중합체로 경화하는 유기 폴리실록산 조성물
EP0735103B1 (fr)	2003-01-08	Adhésifs de contact thermofusibles à base de silicone réticulable par l'humidité
US3629228A (en)	1971-12-21	Non-corrosive siloxane vulcanizable at room temperature
CN101772551B (zh)	2013-05-29	基于有机硅化合物的可交联物质
US4973644A (en)	1990-11-27	Room temperature-curable organopolysiloxane composition
EP0628619A2 (fr)	1994-12-14	Procédé de collage de substrats à l'aide de compositions d'organopolysiloxane à l'état fondu et durcissable par l'humidité
EP0625548A2 (fr)	1994-11-23	Composition d'organopolysiloxane réticulable à température ambiante et méthode pour sa préparation
JP2002531621A (ja)	2002-09-24	水分の存在下に周囲温度から半透明エラストマーに硬化するオルガノポリシロキサン組成物
US3529035A (en)	1970-09-15	High strength silicone elastomers
US5612400A (en)	1997-03-18	Silicone pressure sensitive adhesive compositions and method for making
US4968760A (en)	1990-11-06	Paintable organopolysiloxane compositions which crosslink at room temperature to form elastomers
US5210156A (en)	1993-05-11	Stable, moisture-curable silicone pressure sensitive adhesives
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